Description
Job Location: London, UK
Job Location Type: Hybrid
Job Contract Type: Full-time
Job Seniority Level: Mid-Senior level
Company Overview:
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, ACO®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care.
Description Overview:
In this role, you will manage Regulatory Affairs Projects as required to meet business needs. You will ensure compliance with the existing legislation and regulations for medicines, and assist in any area of Regulatory Affairs at corporate level.
Scope of the Role:
- Lead Regulatory Affairs Projects; providing updates to business and reporting against project plans.
- Develop regulatory strategies for new MAAs and NPD projects, identifying risks and opportunities.
- Complete due diligence on time for any assigned product dossiers, identifying risks and opportunities.
- Manage, execute and co-ordinate new MAA applications/ NPD projects including product name strategy, product information text, review of claims, advertising material and pack design.
- Develop, roll out and maintain relevant internal procedures and best practices.
- Maintain the integrity of regulatory data in relevant databases.
- Interpret and implement legislation; follow changes in national regulations; proactively manage impact of these changes.
Experience Required:
- A scientific degree in a pharmaceutical, chemical or biological discipline.
- 5 years Regulatory Affairs experience ideally within UK or EU OTC including Post Marketing Licence Maintenance activities; creation & submission of MAAs.
- Self-motivated; flexible; open to changing requirements.
- Highly driven with enthusiasm to meet requirements under demanding pressure.
- Project management skills with ability to work autonomously with guidance when required.
- Ability to make decisions; problem solve; prioritise & multi-task effectively.
- Stakeholder management skills essential.
- Continuous improvement & knowledge sharing focused.
Benefits:
We believe our people are our greatest asset. Alongside competitive compensation we offer benefits tailored to supporting you & your family as well as career development opportunities ensuring you feel valued & supported both professionally & personally.
Hybrid Working Approach:
We love our offices & appreciate their setting for collaboration but also value remote work flexibility allowing two days a week from home in many roles.
Recognition:
We are proud recipients included in Forbes list "America's Best Employers by State 2024".
Application Process:
Applicants please note: To apply for this position please click the APPLY button at bottom of application (The SAVE button only saves profile information but does not submit an application). Thank you.
Equal Opportunity Employer Statement:
We are an equal opportunity employer. All qualified applicants will receive consideration without regard race color religion sex sexual orientation gender identity national origin disability status protected veteran or other characteristics protected by law. Our full Equal Employment Opportunity Affirmative Action Policy Statement is available on main career site English Spanish provided accessible forms persons disabilities.
Additional Information:
#DIV #weareperrigo
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